instant free hand sanitizer
Generic: alcohol
Labeler: travel retail global incDrug Facts
Product Profile
Brand Name
instant free hand sanitizer
Generic Name
alcohol
Labeler
travel retail global inc
Dosage Form
GEL
Routes
Active Ingredients
alcohol .75 mL/mL
Manufacturer
Identifiers & Regulatory
Product NDC
77129-000
Product ID
77129-000_08a251f6-627c-d24a-e063-6394a90a3b3e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2020-05-10
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
77129000
Hyphenated Format
77129-000
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
instant free hand sanitizer (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .75 mL/mL
Packaging
- 50 mL in 1 BOTTLE (77129-000-50)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "08a251f6-627c-d24a-e063-6394a90a3b3e", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["1305100"], "spl_set_id": ["a3ffa72b-b7d4-463a-a880-66081f16bd1a"], "manufacturer_name": ["Travel Retail Global Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (77129-000-50)", "package_ndc": "77129-000-50", "marketing_start_date": "20200510"}], "brand_name": "INSTANT FREE HAND SANITIZER", "product_id": "77129-000_08a251f6-627c-d24a-e063-6394a90a3b3e", "dosage_form": "GEL", "product_ndc": "77129-000", "generic_name": "ALCOHOL", "labeler_name": "Travel Retail Global Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "INSTANT FREE HAND SANITIZER", "active_ingredients": [{"name": "ALCOHOL", "strength": ".75 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200510", "listing_expiration_date": "20261231"}